Environment, mitochondria, and Parkinson's disease

被引:170
作者
Sherer, TB [1 ]
Betarbet, R [1 ]
Greenamyre, JT [1 ]
机构
[1] Emory Univ, Dept Neurol, Atlanta, GA 30322 USA
关键词
neurodegeneration; oxidative stress; excitotoxicity; pesticides;
D O I
10.1177/1073858402008003004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Parkinson's disease (PD) is a common and disabling neurodegenerative disease marked by progressive motor dysfunction, which results from selective degeneration of the nigrostriatal pathway. Epidemiological studies indicate that exposure to pesticides, rural living, farming, and drinking well water are associated with an increased risk of developing PD. Rare cases of PD are caused by mutations in nuclear genes, and there is increasing evidence for susceptibility genes that alter disease risk. Parkinson's disease is also associated with a systemic defect in mitochondrial complex I activity. Animal models indicate that exposure to inhibitors of mitochondrial complex 1, including pesticides, is sufficient to reproduce the features of PD, but genetic factors clearly modulate susceptibility. Complex I defects may result in oxidative stress and increase the susceptibility of neurons to excitotoxic death. In this way, environmental exposures and mitochondrial dysfunction may interact and result in neurodegeneration.
引用
收藏
页码:192 / 197
页数:6
相关论文
共 44 条
[11]  
Gorell JM, 1999, NEUROTOXICOLOGY, V20, P239
[12]   Response: Parkinson's disease, pesticides and mitochondrial dysfunction [J].
Greenamyre, JT ;
Betarbet, R ;
Sherer, T ;
Panov, A .
TRENDS IN NEUROSCIENCES, 2001, 24 (05) :247-247
[13]   Bioenergetics and glutamate excitotoxicity [J].
Greene, JG ;
Greenamyre, JT .
PROGRESS IN NEUROBIOLOGY, 1996, 48 (06) :613-+
[14]   Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease [J].
Gu, M ;
Cooper, JM ;
Taanman, JW ;
Schapira, AHV .
ANNALS OF NEUROLOGY, 1998, 44 (02) :177-186
[15]   1-METHYL-4-PHENYLPYRIDINIUM (MPP+) INDUCES NADH-DEPENDENT SUPEROXIDE FORMATION AND ENHANCES NADH-DEPENDENT LIPID-PEROXIDATION IN BOVINE HEART SUBMITOCHONDRIAL PARTICLES [J].
HASEGAWA, E ;
TAKESHIGE, K ;
OISHI, T ;
MURAI, Y ;
MINAKAMI, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (03) :1049-1055
[16]  
Hensley K, 1998, J NEUROCHEM, V71, P2549
[17]   UPTAKE OF MPP(+) BY DOPAMINE NEURONS EXPLAINS SELECTIVITY OF PARKINSONISM-INDUCING NEUROTOXIN, MPTP [J].
JAVITCH, JA ;
SNYDER, SH .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1984, 106 (02) :455-456
[18]   Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism [J].
Kitada, T ;
Asakawa, S ;
Hattori, N ;
Matsumine, H ;
Yamamura, Y ;
Minoshima, S ;
Yokochi, M ;
Mizuno, Y ;
Shimizu, N .
NATURE, 1998, 392 (6676) :605-608
[19]  
Koller WC., 1997, MOVEMENT DISORDERS N, P125
[20]   CHRONIC PARKINSONISM IN HUMANS DUE TO A PRODUCT OF MEPERIDINE-ANALOG SYNTHESIS [J].
LANGSTON, JW ;
BALLARD, P ;
TETRUD, JW ;
IRWIN, I .
SCIENCE, 1983, 219 (4587) :979-980